JP6749622B2 - Subcutaneous tissue therapy - Google Patents

Description

This invention is for a cervical head that is configured by dividing the skull surface from the neck to the frontal muscle or temporal muscle centering on the occipital bone into four division zones and maintaining the width of each division zone. By using the bifurcated operation part, it is possible to easily give immunity by stimulating the subcutaneous tissue of the four division zones from the neck to the frontal muscle or the temporal muscle without requiring specialized skills. The present invention relates to a surgical instrument for subcutaneous tissue therapy.

Conventionally, a wide variety of muscles, nerves, and lymph vessels run from the cervical region to the frontal region or the temporal muscle, and especially in oriental medicine, a meridian that connects scattered and concentrated pots (acupuncture points) runs. Stimulation of nerves, lymph vessels, and meridians has been used as a medical method to obtain medical effects such as improvement of blood flow, relaxation effects to relieve mental and physical tension, and massage effects such as kneading. For this reason, there is so-called acupressure therapy in which the meridian and nerve muscles and muscles of such a portion are stimulated and treated by using the operator's fingers.

This has the drawback that the effect given to the patient depends on the skill of the practitioner, and therefore there is a drawback that many practitioners cannot request uniform skill therapy, and the procedure is performed because of long-term simple shiatsu and rubbing work. The person has a heavy physical load, and requires long-term practice training to train and acquire a certain level of acupressure skills.

Therefore, in order to eliminate these drawbacks, a technique has been devised in which acupressure devices configured in a certain shape are used to acupressure the pots and predetermined muscles of the human body with tools instead of the fingers of the practitioner.

Therefore, it is necessary for the acupressure device to have a device structure of a certain shape that is suitable for acupressure points and that can be used for pressing a finger, and many design and shape patents have been applied for the shape of the acupressure device (for example, refer to Patent Document 1). Registered or registered.

JP, 10-43270, A

In this way, the acupressure device shaped into a constant shape is, for example, an object equivalent to acupressure while aiming an effect equal to that of the acupressure while controlling the force by pressing the protruding portion of the cloud-shaped plate against the affected part. The molded body may be a molded body modeled according to the acupressure point, or may be a molded body formed with a large number of protrusions so as to be pressed against a plurality of affected areas at the same time for medical treatment in a short time.

Moreover, as a usage pattern of the device, a plurality of finger holes are formed in the central part of the device body, a finger is inserted into the finger hole, and the entire device is grasped by the palm part, and the device protrusion of a certain shape is pressed against the affected area and pressed. The stress is effectively propagated from the device to the affected area.

However, all of these acupressure devices have advantages and disadvantages, and even if the acupressure device body is grasped by the palm part and pressed against the affected area, the pressing force of the practitioner's palm part is not effectively transmitted to the device body, and thus the pressing stress is generated. However, it has a drawback that it does not reach the affected area sufficiently and that it requires extra force for the operation, which increases the physical load on the operator and makes it difficult to perform the operation for a long time.

Further, in order to perform stimulation therapy to the skull in the head, since the shape of the acupressure tool is not a structure that can be commonly used on almost all surfaces of the head, there are many acupressure tools having different shapes depending on the head position of the affected area. It is necessary to prepare all of them, and there are drawbacks such as acupressure therapy being complicated and the therapy equipment being expensive.In the end, a single surgical instrument can be used in a wide range from the back of the head to the top of the head, easily and with as little physical as possible. There was nothing that could perform effective subcutaneous tissue stimulation under load.

In order to solve the above-mentioned conventional problems, the present invention provides a surgical instrument main body including a grip portion, a bifurcated cervical operation portion formed at the tip of the grip portion, and a grip portion formed at the rear end of the grip portion. In addition, the bifurcated operation part for the cervical head is composed of a combination of a lower projection located closer to the neck and an upper projection located closer to the crown at the time of operation. The anterior end of the superior process and the anterior end of the inferior process of the part are formed so that the skull surface can be placed over each of the divided zones when the skull surface is divided into four divided zones from the occipital region to the frontal region. Of the four sections divided into the head, the first section that divides the skull surface is the suboccipital muscle group portion that covers the skull base between the left and right temporal bones in layers, and the lower term line in the headline. Assuming a curved surface area located between the upper term line and the upper term line in the head line, the second zone that divides the skull surface is the occipital muscle part that covers the posterior half of the calvaria between the left and right temporal bones. Assuming a curved surface area defined by the aponeurosis and the area between the superior line of the head line and the frontal muscle and the areas of the left and right temporal bones, the skull surface is divided. The third segmented zone is assumed to be a curved surface area defined by the frontal muscle portion covering the anterior half of the calvaria between the left and right temporal bones, and the fourth segmented zone that divides the skull surface covers the left and right temporal bones. Assuming a curved surface area divided by the temporal muscle part, the distance between the front ends of the upper and lower protrusions of the bifurcated treatment part is lower than the boundary line between the first division zone and the second division zone. The intervals in which the protrusions contact the meridians of the first section band, the upper projections contact the meridians of the second section band, the intervals contact the front and back meridians scattered in the front-rear direction in the area of the second section band, and the second section band. And a third section band, while the upper projection is displaced along the boundary line, the lower projection contacts the meridian of the third section band, the upper projection along the boundary line between the second section band and the fourth section band. It is intended to provide a subcutaneous tissue therapy surgical instrument characterized by satisfying the respective intervals such as the intervals at which the lower protrusion abuts on the meridian of the fourth section band while displacing.

Further, the lower protrusion of the bifurcated treatment portion is configured to project longer in the tip direction than the upper protrusion, and the front end of the upper and lower protrusions of the bifurcated treatment portion is separated from the first section by the second section. An interval in which the longer downward projection abuts on the meridian of the first section and the shorter upper projection abuts the meridian of the second section on the boundary between the section and the front and rear of the area of the second section. The abutment with the front and back meridians scattered in the direction, while the shorter upper projection is displaced along the boundary line between the second section band and the third section band, the longer lower projection contacts the meridian of the third section band. Satisfies each interval such as the contacting interval, the interval at which the longer lower projection abuts the meridian of the fourth partitioning band while displacing the shorter upper projection along the boundary line between the second partitioning band and the fourth partitioning band. It is characterized by doing.

In addition, the upper protrusion of the bifurcated treatment portion is projected along the axial direction of the grip portion, and the lower protrusion is inclined about 40° to 60° with respect to the axial direction of the grip portion. To do.

In addition, the upper and lower projections of the bifurcated treatment portion are flat, and the flat leading edge is formed by recessing the central portion of the wall thickness, thereby forming left and right projecting edge portions on both flat sides.

Further, when the bar-shaped gripping part between the bifurcated operation part and the grip part is grasped as the width of the palm grip part of the practitioner, both widthwise end surfaces of the palm grip part are in close contact with the bifurcated operation part and the grip part. It is characterized in that it is configured to.

Further, the bifurcated portion is characterized in that it is gradually sharpened toward the distal end, and the distal end portion is rounded in plan view and gradually thinned in side view.

Further, the functional surface of the bifurcated treatment portion formed at the front end of the grip portion is characterized by being formed into a rough surface so that sliding friction is large.

In addition, the main body of the treatment device is made of resin, and is configured so that a weight feeling can be maintained during the treatment work and a stable treatment can be performed.

According to the invention of claim 1, since the bifurcated operation part is basically operated by tracing the spherical surface of the skull while pressing and stimulating the affected part, the direction in which the pressing stress is most applied to the skull is turned down. The vertical direction of the head of the sleeping patient, that is, the horizontal direction of the head in the standing position of the patient is divided into 4 sections, and the 4 sections are subjected to subcutaneous tissue stimulation therapy from the posterior surface of the skull to the crown. You can

Here, when the skull is divided into four division zones from the occipital region to the frontal region, the first division zone that divides the surface of the skull is the suboccipital muscle group portion that covers the skull base between the left and right temporal bones in layers, and Assuming a curved surface area located between the lower term line of the nodal line and the upper term line of the head nodal line, the second zone that divides the skull surface is the second half of the calvaria between the left and right temporal bones. In the occipital muscle portion and cap-shaped aponeurosis portion that cover, and a surface curved area partitioned by each area of the area between the superior line of the head line and the frontal muscle and the area of the left and right temporal bones. Assuming that the 3rd division zone that divides the skull surface is the 4th division zone that divides the skull surface, assuming a surface curved area divided by the frontal muscle part that covers the anterior half of the calvaria between the left and right temporal bones. Assumes a curved surface area defined by the temporal muscle portion covering the left and right temporal bones.

When the surgical instrument main body is vertically pressed against each of these segment bands to apply a pressing stress in the axial direction of the grip, the pressing stress is evenly transmitted to the affected area via the upper and lower projections, and It has the effect of stimulating the meridians of the subcutaneous tissue.

That is, in the present invention, the tip of the upper and lower projections is in close contact with the affected part of the head even when the input direction is perpendicular to the prone head substantially spherical body, and the bifurcated treatment part capable of exerting stimulation stress to the maximum extent possible. It is characterized by the structure.

Also, when stimulating the 4-section zone of the head of a patient lying prone in the vertical direction from the posterior surface of the prone skull, the surface shape of the head is far from the main body of the surgical instrument along the lower edge line of each zone. ..

That is, if the upper and lower protrusions have the same length, the lower protrusions that are directed toward the lower edge of each division band are aligned with the upper edge line of each division band if the surgical instrument main body is in a vertical posture with respect to the four division bands. It will be located farther than the upward projection that is facing.

Therefore, since the projections necessarily contact the affected part of the skull evenly, the lower projection is necessarily formed longer than the upper projection.

As a shape conforming to such a logic, in the invention according to claim 2, the lower projection of the bifurcated operation portion is configured to project longer in the distal direction than the upper projection, that is, the bifurcated operation for the neck and head. Part of the skull is combined with an inferior protrusion located farther from the skull and an upper protrusion located closer to the skull, and as a result, a rod-shaped gripping portion is pressed vertically against each section of the prone skull. Thus, the upper and lower protrusions having different tip lengths have the effect of being able to apply the most effective and uniform stimulus to subcutaneous cells at different positions.

In addition, the distance between the front ends of the upper and lower projections of the bifurcated treatment part can be commonly used for the four section bands, so that the longer one of the lower projections straddles the boundary line between the first section band and the second section band. Is the interval at which the shorter upper projections contact the meridians of the first section band respectively contact the meridians of the second section band, the intervals at which they contact the front and rear meridians scattered in the respective front-rear directions within the area of the second section band, the second section An interval in which the shorter lower protrusion abuts the meridian of the third segment while displacing the shorter upper protrusion along the boundary line between the strip and the third segment, and the second segment and the fourth segment Since the shorter upper protrusion is displaced along the boundary line and the longer lower protrusion abuts on the meridian of the fourth section zone, the front end interval satisfying each interval is configured, so that one treatment device is provided. Only by doing so, it is possible to perform the necessary stimulation of the subcutaneous tissue of almost the entire skull, and it is possible to improve the efficiency of the operation and at the same time, a certain level of operation technique common to many practitioners without requiring special skill. Can be given to patients.

According to the invention of claim 3, when the main body of the practitioner is vertically pressed against each of the division bands to apply a pressing stress in the axial direction of the gripping portion, the pressing stress is more evenly applied to the affected area via the upper and lower projections. It is effective in stimulating the meridians of the subcutaneous tissue at the upper and lower edges of each zone.

According to the invention of claim 4, there is an effect that a large amount of skin contacts on the surface of the skull at the time of operation increases frictional resistance, and a stable pressing force can be applied to the affected area.

According to the fifth aspect of the present invention, the width of the palm gripping portion which is rounded for gripping the rod-shaped gripping portion fits tightly between the bifurcated operation portion and the gripping portion, so that the gripping stress at the palm gripping portion is sufficiently increased. It can be exerted and the pressing force to the affected area can be transmitted as desired by the practitioner through the operation device, and there is an effect that a reliable subcutaneous tissue stimulation can be performed on the affected area.

According to the sixth aspect of the present invention, the bifurcated treatment portion can be accurately placed at the treatment effective point of the affected area and effectively functions on the affected subcutaneous tissue without giving unnecessary excessive stimulation to the affected area. There is an effect that can be made.

According to the invention of claim 7, the functional surface of the bifurcated treatment portion formed at the front end of the grip portion is formed as a rough surface so that the sliding friction is large, so that the treatment instrument is pressed against the surface of the affected portion. In this case, there is no risk of slipping and slipping, and there is an effect that the operation device can be reliably positioned in the affected subcutaneous tissue and the operation operation work can be performed efficiently and functionally.

According to the invention of claim 8, the material of the surgical instrument main body is made of resin, and the surgical instrument main body is configured to hold a feeling of weight during the surgical operation so that a stable surgical operation can be performed. At the same time, there is an effect that the operation operation can be easily performed.

It is a front view of the subcutaneous tissue treatment operation instrument concerning this embodiment. It is a front view of the subcutaneous tissue treatment operation instrument concerning this embodiment. It is a front view and a top view of a subcutaneous tissue treatment operation instrument concerning this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is a front perspective view at the time of dividing the skull surface. It is a rear perspective view when the surface of the skull is divided. It is a front view at the time of dividing the skull surface. It is a rear view when the skull surface is divided. It is a side view at the time of dividing the skull surface. It is a front enlarged view of the bifurcated operation part of the subcutaneous tissue therapy operation device concerning this embodiment. It is a front view, a top view, and a sectional view showing a modification of a subcutaneous tissue treatment operation instrument concerning this embodiment. It is a perspective view and a top view showing a modification of a subcutaneous tissue treatment operation instrument concerning this embodiment. It is a perspective view and a top view showing a modification of a subcutaneous tissue treatment operation instrument concerning this embodiment. It is explanatory drawing which shows the holding|grip state of the subcutaneous tissue therapy operation instrument which concerns on this embodiment. It is explanatory drawing which shows the holding|grip state of the subcutaneous tissue therapy operation instrument which concerns on this embodiment. It is explanatory drawing which shows the holding|grip state of the subcutaneous tissue therapy operation instrument which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment. It is explanatory drawing which shows the usage example of the subcutaneous tissue therapy operation apparatus which concerns on this embodiment.

The gist of the present invention is to configure a surgical instrument main body with a grip portion, a bifurcated procedural operation portion for the head of the neck formed at the tip of the grip portion, and a grip portion formed at the rear end of the grip portion. The bifurcated procedural part is composed of a combination of a lower protrusion located closer to the neck and an upper protrusion located closer to the parietal region during operation. The anterior end is divided into 4 sections from the occipital region to the forehead, and the front end is formed with an interval that can be placed over both edge lines of each division band. Moreover, the skull is divided from the occipital region to the frontal region. Of the four divided zones, the first divided zone that divides the surface of the skull is the suboccipital muscle group portion that covers the skull base between the left and right temporal bones in layers, and the lower term line and the head term line in the head term line. Assuming a curved surface area that is located between the upper and the medial superior line, the second division zone that divides the surface of the skull is the occipital muscle portion that covers the posterior half of the calvaria between the left and right temporal bones and the cap aponeurosis. A third section in which the skull surface is sectioned by assuming a surface-curved area that is divided into areas, that is, the area between the upper line of the head line and the frontal muscle, and the areas of the left and right temporal bones. The band is assumed to be a curved surface area defined by the frontal muscle part covering the anterior half of the calvaria between the left and right temporal bones, and the fourth segmented zone that divides the surface of the skull is the temporal muscle covering the left and right temporal bones. Assuming that the curved surface area is divided into parts, the interval between the front ends of the upper and lower protrusions of the bifurcated treatment part is such that the lower protrusion is first across the boundary line between the first section band and the second section band. The intervals at which the upper protrusions abut the meridians of the section bands, respectively, the intervals at which the upper protrusions abut the front and back meridians scattered in the respective front-rear directions within the area of the second sections, the second section band and the third section band. The lower protrusion while displacing the upper protrusion along the boundary line with and the lower protrusion while displacing the upper protrusion along the boundary line between the second segment band and the fourth segment band. It is an object of the present invention to provide a subcutaneous tissue therapy surgical instrument characterized by satisfying each interval, such as the interval at which the protrusion abuts the meridian of the fourth section band.

The subcutaneous tissue therapy device according to the present invention is fundamentally different from a device that simply "presses" and "rubs" to obtain a massage effect like a general massage device. By "pushing", "turning", and "pulling" under the "circumstance", the tissue underneath is compressed without escaping from the pressing direction, and stretch extension of the subcutaneous tissue of the head to activate the tissue, lymph, muscle ligament, etc. It is a device dedicated to pressing.

The scalp is divided into five parts: skin, connective tissue, aponeurosis, sparse ring-like connective tissue and skull periosteum, and the skin is further divided into epidermal tissue, dermal tissue and subcutaneous tissue.

The epidermal tissue consists of stratum corneum, granular layer, spinous layer and basal layer, and dermal tissue consists of appendages such as papillary layer, subpapillary layer, reticular layer, blood vessels, nerves, sebaceous glands and sweat glands, and subcutaneous tissue contains a large amount of fat and capillaries. It is a tissue having blood vessels and has a role of protecting the tissue by a cushion function.

Most of the parietal region under the head of the head is covered with a cap-like aponeurosis, and the connective tissue is thinner and stiffer than other parts of the human body, so finger pressure from fingers is transmitted only to the skin.

However, if a subcutaneous tissue therapy device with a large friction coefficient is used, unlike pressing only on the skin, the pressing force of the epidermal tissue can be applied in a stable state in which the subcutaneous tissue is grasped so as to grasp the skin surface of the affected area without slipping. The effect of manipulative treatment is improved by applying a pressure stimulus to useful functional parts of the human body such as blood vessels, nerves and sweat glands.

That is, on the functional surface where the bifurcated treatment part comes into contact with the skin, by increasing the contact area and forming a rough surface to increase the frictional resistance, "grasp and pull the scalp together with the subcutaneous tissue", in short The skin is stretched to the maximum extent and stretched so that there is no escape of subcutaneous tissue cells, and the cap aponeurosis between the skin and the skull and the stiff tissue of the frontal, occipital, and temporal muscles It can be said that it is a device that can be rotated and pushed after being pulled to the maximum like crushing.

Hereinafter, specific embodiments will be described in detail with reference to the drawings. 1 and 2 are front views of a subcutaneous tissue therapy surgical instrument according to the present embodiment, and FIGS. 3(a) and 3(b) are front views and plan views of the subcutaneous tissue therapy surgical instrument according to the present embodiment. 4 to FIG. 7 and FIG. 20 to FIG. 22 are explanatory views showing an example of use of the subcutaneous tissue therapy operation device, FIG. 8 to FIG. 12 are explanatory views when the head is divided into division zones as the treatment area, and FIG. Moreover, the front view which expanded the front-end of the upper and lower protrusion of the curved operation part, FIGS. 14-16 is explanatory drawing which shows the modification of the subcutaneous tissue therapy operation device which concerns on this embodiment, and FIGS. 17-19 is a palm of a practitioner. It is explanatory drawing which shows the state which hold|gripped the subcutaneous tissue therapy operation device by.

[1. Embodiment)
In the subcutaneous tissue therapy surgical instrument A according to the present invention, as shown in FIGS. 1 and 3, the surgical instrument main body 1 has a rod-shaped or narrow flat plate-shaped grip portion 2 and a neck head formed at the tip of the grip portion 2. It is composed of a bifurcated treatment part 3 and a grip part 4 formed at the rear end of the grip part 2.

Moreover, the bifurcated operation part 3 for the cervical head of the operation device body 1 is formed by the combination of the lower protrusion 6 located closer to the neck and the face and the upper protrusion 5 located closer to the crown during the operation. I am configuring. That is, the practitioner main body 1 is formed in a substantially Y shape as shown in FIGS. 1 and 3, and a thick portion extending in the central portion in the Y shape is used as a grip portion 2, and A bifurcated operation part 3 is a part that bifurcates and extends.

As shown in FIGS. 4 to 6, the position where the upper protrusion front end 5a and the lower protrusion front end 6a of the bifurcated treatment part 3 are in contact with each other is as shown in FIGS. It is divided into four division bands, that is, a second division band C2, a third division band C3, and a fourth division band C4, and the position is located between the meridians distributed in a mesh shape in the surface curved area of each division band. .. That is, the interval between the front end 5a of the upper protrusion and the front end 6a of the lower protrusion of the bifurcated treatment part 3 is a common interval connecting the meridians (pots) present in each section band.

The reason is that, as shown in FIGS. 4 to 6, the bifurcated operation part 3 is basically operated by tracing the spherical surface of the skull while pressing and stimulating the affected part. It is desired to have a bifurcated treatment part structure for maximizing the pressing force so that the pressing stress is applied in a direction perpendicular to the spherical surface as much as possible.

In general, the meridian as an operation point is a thicker tissue side than a hat-shaped aponeurosis of a thin tissue covering almost the entire area of the neck and the face, that is, the parietal region rather than the parietal region. It is abundant in the temporal muscles of the head, the frontal muscles of the frontal region, and multiple muscle groups in the lower occipital region. Further, the head surface reaches the temporal region, the frontal region, and the lower occipital region through a curved portion having a higher bending rate as it gets farther from the parietal region.

That is, as shown in FIG. 8 to FIG. 12, in the present invention, the skull is divided into four division zones from the occipital region to the frontal portion in order to perform the treatment in accordance with the appropriate treatment point, and the skull surface is divided into the first division zone. C1 is the suboccipital muscle group M1 part that covers the skull base B1 between the left and right temporal bones B4, B4′ in a layered manner, and includes the lower term line D1 in the head term line and the upper term line D2 in the head term line. The second zone C2 that divides the surface of the skull assuming a surface curved area located between is a occipital muscle M3 portion covering the posterior half of the calvaria B2 between the left and right temporal bones B4 and B4′ and the aponeurosis. Assuming a surface curved area defined by the M2 portion and the area between the upper term line D2 in the head term line and the frontal muscle M4, and the areas of the left and right temporal bones B4, B4′, The third zone that divides the skull surface assumes a surface curved area that is divided by the frontal muscle M4 portion that covers the anterior half of the calvaria B3 between the left and right temporal bones B4 and B4′, and divides the skull surface. The 4-section zone C4 has a shape assuming a surface curved area defined by the temporal muscles M5 and M5′ that cover the left and right temporal bones B4 and B4′.

In particular, in this embodiment, as shown in FIGS. 1 and 3, a bifurcated procedural portion 3 for the cervical head is provided with a lower protrusion 6 and a head which are located closer to the cervical portion or the like during the treatment. It is configured by a combination of upper protrusions 5 located closer to the top.

The bifurcated treatment portion 3 is formed so that the interval L between the front end 5a of the upper protrusion and the front end 6a of the lower protrusion is a common interval connecting the meridians (pots) present in each section band.

Specifically, the interval L between the front end 5a of the upper protrusion 5 and the front end 6a of the lower protrusion of the bifurcated treatment part 3 is basically formed in accordance with the scale of Oriental medicine, for example, the head of a patient. It can be formed according to the size and shape of the part, for example, the interval between common meridians existing for each physical characteristic of a patient such as for children and adults, for women and men. The length L of the interval L between the front end 5a of the upper protrusion and the front end 6a of the lower protrusion of the bifurcated treatment part 3 in this embodiment is about 4 to 7 cm, preferably 5 to 6 cm.

Here, the bifurcated operation part 3 in the subcutaneous tissue therapy operation device A is not only a bifurcated operation part formed on the operation device main body 1 but also a vertical direction at the tip of the grip portion 2 of the operation device main body 1. Also, a plurality of strut-shaped treatment portions such as four-sided, five-sided, and so on are formed, and a plurality of straddle-shaped treatment portions of the plurality of strut-shaped treatment portions are also included at intervals corresponding to each section zone.

That is, it is sufficient that the bifurcated treatment portion 3 of the present invention is included in a plurality of strut treatment portions in the treatment device body 1 as shown in FIG. 2A shows two bifurcated treatment parts 3 and 3'in the trifurcated treatment part, and FIG. 2B shows three bifurcated treatment parts 3 and 3'in the trifurcated treatment part. 3'and 3'' are included.

Specifically, as shown in FIG. 2A and FIG. 2B, when a plurality of protrusions are formed so as to be continuous in the vertical direction at the tip of the grip portion 2 in a front view, among the plurality of protrusions, In the two vertically adjacent projections, if the spacing between their front ends is a common spacing L that connects the meridians (pots) present in each section band, then these two projections 5, 6 and the projections 5′, 6 The projections 5 ″ and 6 ″ are the upper and lower projections 5 and 6 of the present invention, respectively, and constitute the bifurcated operation part 3.

Further, as shown in FIG. 10, the functional surface of the bifurcated treatment portion 3 formed at the front end of the grip portion 2 is formed as a rough surface 30 having a large frictional resistance.

As a method of forming such a rough surface 30, for example, the surface of the practitioner body 1 is subjected to sandblasting or powder-particle coating treatment, or the practitioner body 1 itself is subjected to 3D printer lamination molding or powder-particle dispersion hardening. By molding, a fine concavo-convex surface can be formed on the surface of the treatment device body 1.

In performing the sand blasting process, a fine grinded surface, for example, a roughened surface having a gauze pattern is formed by rubbing the surface of the practitioner body 1 with a grindstone for polishing, sandpaper, or a file.

In addition, when performing the powdery particle coating treatment, a fine uneven surface is formed by spraying and adhering fine powdery particles such as glass powder or sand particles onto the surface of the treatment device body 1.

In addition, when laminating the practitioner body 1 with a 3D printer, for example, a direction orthogonal to the axis of the grip portion, specifically, a virtual plane formed by the front end faces of the upper protrusion 5 and the lower protrusion 6 is orthogonal. By laminating resin or the like in the vertical direction, fine irregularities along the vertical direction are formed on the front end faces of the upper and lower protrusions 5 and 6.

Further, when the treatment device main body 1 is dispersion-hardened and molded, the uncured resin in which fine powder particles are dispersed is poured into the mold of the treatment device main body 1 and cured, whereby the treatment device main body 1 Fine particles are exposed on the outer surface to form a fine uneven surface. The particle size of the powder or granular material used for the powder or granular material coating treatment or the powder or granular material dispersion hardening is not particularly limited as long as the rough surface 30 is formed on the surface of the treatment device body 1.

Further, the rough surface 30, which is the functional surface of the bifurcated portion 3 formed by the above method, has a surface roughness of Ra 10 μm to 35 μm, more preferably Ra 15 μm to 30 μm. It is possible to reliably obtain the frictional resistance force of the portion 3 with respect to the scalp surface.

The functional surface of the bifurcated treatment part 3 is not particularly limited as long as the frictional resistance is large. For example, an elastic material (for example, vinyl resin) formed separately or a cap having a rough surface is used. It is also possible to cover the surfaces of the upper and lower projections 5 and 6 of the bifurcated part 3 with the shaped parts. That is, the functional surface of the bifurcated treatment part 3 may be configured by a cap-shaped part having a large frictional resistance, which is attachable to and detachable from the upper and lower protrusions 5, 6.

Here, the functional surface of the bifurcated treatment part 3 is a surface where the front end surface of the upper protrusion 5 and the front end surface of the lower protrusion 6 contact the scalp surface, respectively. Each of the surface area of the front end face of the upper protrusion 5 and the lower projection 6, 5mm ² ~30mm ^2, more preferably is formed to have a 10 mm ² 25 mm ^2.

With such a configuration, when the bifurcated operation part 3 is applied to the scalp surface, the front end surfaces of the upper and lower projections 5 and 6 are brought into surface contact with the scalp surface, thereby increasing the friction resistance surface. It is possible to prevent damage to the scalp surface due to the front ends of the upper and lower protrusions 5 and 6, and to prevent the surgical instrument main body 1 from sliding on the scalp surface. In addition, the bifurcated operation part 3 can grasp the scalp surface together with the subcutaneous tissue in the deep part of the scalp over a wide area, and when the operation instrument main body 1 is pushed and rotated, the affected tissue can be reliably released.

Further, the lower protrusion 6 of the bifurcated treatment part 3 is formed in a shape projecting longer in the distal direction than the upper protrusion 5 as shown in FIG. That is, when pressing the rod-shaped grip portion 2 in the direction perpendicular to the surface of the skull, the upper and lower projections 5 and 6 have different lengths to the front end as shown in FIG. With the same pressing stress of the protrusions, it is possible to apply a stimulation as even as possible to subcutaneous cells at different positions.

That is, as shown in FIGS. 4 to 7, since the skull surface divided into the four division bands is a spherical surface, the skull surface was oriented perpendicular to the skull surface in order to conform to the unevenness due to the curved shape of the skull. With respect to the pressing direction of the grip portion 2, the two affected areas at regular intervals in each section have a lower distance (rear) and a longer distance than the upper (front) when viewed from the grip portion 2.

Therefore, the length of the upper and lower projections 5 and 6 is made longer as described above so that the surgical pressing force is evenly applied to the two affected areas at the upper and lower edges of the sectioned band.

In particular, the suboccipital muscle group M1 portion in the surface curved area of the first section band C1 in which the meridians (pots) as the treatment points are densely distributed, and the frontal muscle M4 in the surface curved area of the third section band C3 When pressing the portion and the temporal muscle M5 portion in the surface curved area of the fourth section band C4, a bifurcated operation is performed on the cap aponeurosis M2 portion in the surface curved area of the second section band C2. The front end 5a of the upper protrusion 5 of the portion 3 is arranged as a fulcrum of the pallet, and the front end 6a of the lower protrusion 6 is used as an action point to apply a pressing force to the affected parts of the suboccipital muscle group M1, the frontal muscle M4, and the temporal muscle M5. By making it act, the meridians distributed in the curved surface area of each zone can be surely pressed and stimulated.

The relationship between the lengths of the upper and lower protrusions 5 and 6 (distance from the forked valley portion to the front end of each protrusion in the axial direction of the gripping portion) is defined by the bifurcation expansion angle of the upper and lower protrusions 5 and 6 ( It depends on the inclination angle), but as an example, the length of the upper protrusion: the length of the lower protrusion = 1:1 to 1.5.

Further, as shown in FIG. 3, the subcutaneous tissue therapy surgical instrument A according to the present invention has the upper projection 5 of the bifurcated surgical treatment section 3 in the surgical instrument main body 1 in the direction of the axis E of the grip portion 2 (broken line in FIG. 3 ). ), and the lower protrusion 6 is provided with an inclination angle of about 40° to 60° with respect to the direction of the axis E of the grip portion 2.

More specifically, the upper protrusion 5 has a front end 5a of the upper protrusion 5 at one end of the upper protrusion axis E1 that extends at a predetermined distance from the axis E and extends parallel to the axis C of the grip portion 2 in the surgical instrument body 1. It is formed so that.

On the other hand, in the treatment device main body 1, the lower protrusion 6 has the same tip end direction as the front end 5a of the upper protrusion 5, and extends at an inclination angle of about 40° to 60° from the substantially central portion E1a of the upper protrusion axis E1. The tip of the lower protrusion axis E2 is formed to be the front end 6a of the lower protrusion 6.

With such a configuration, as shown in FIGS. 4 to 7, the pressing stress when pressing the rod-shaped gripping portion 2 in the vertical direction with respect to the surface of the skull is equal to or higher than the middle portion of the axis E of the gripping portion 2 or above. The pressing force components are substantially the same that are decomposed from the substantially central portion E1a of the projection axis E1 toward the front ends 5a and 6a of the upper and lower projections 5 and 6, respectively.

That is, the lower protrusion 6 is formed with an inclination of about 40° to 60° from the substantially central portion E1a with respect to the upper protrusion axis E1 which is the direction of the pressing stress of the upper protrusion 5 according to the spherical surface of the skull. The pressing stress of the upper protrusion axis E1 is a substantially uniform pressing force component divided into two parts from the substantially central portion E1a.

As a result, when the subcutaneous tissue therapy apparatus A presses the rod-shaped gripping portion 2 in the direction perpendicular to the surface of the skull, the upward projection 5 exerts a pressing force component in the direction perpendicular to the surface of the skull. On the other hand, the lower protrusion 6 can apply a force component substantially the same as the force component of the upper protrusion 5 to the spherical surface of the skull in an inclined direction, so that the upper and lower edges of the sectioned band can be separated from each other. A more uniform pressure is applied to the affected area.

In addition, the front end intervals of the upper and lower projections 5 and 6 are long across the boundary line (upper line D2) between the first divisional band C1 and the second divisional band C2 so that they can be commonly used for the four divisional bands. The lower protrusions 6 contact the meridians of the first section C1 and the shorter upper protrusions 5 contact the meridians of the second section C2, respectively, and the front and rear meridians scattered in the front-rear direction in the area of the second section. , The interval at which the longer lower projection abuts the meridian of the third section band while displacing the shorter upper projection along the boundary line D3 between the second section band and the third section band, the second A front end interval that satisfies each interval, such as an interval at which the shorter lower protrusion abuts the meridian of the fourth segment while displacing the shorter upper protrusion along the boundary line D4 between the segment band and the fourth segment band. I am trying.

Here, the names of the respective parts such as the skull and the muscles covering the skull are defined as shown in FIGS. 8 to 11, and the terms of the names of the respective parts used in the present specification are as follows. Is defined as
・Skull-The bone that supports the facial structure and protects the brain from the outside, and is formed by stitching 22 bones-Cranial crown-The bone of the round part of the upper half of the skull-The skull base- Bone of the lower half of the head of the skull-Cranial nodules-regions that form the upper and lower nodules in the upper and lower parts, respectively-Upper nodules-The occipital plane of the calvaria in the ridge of the occipital bone The horizontal line running toward the mastoid on the boundary between the and the plane of the base of the skull and the lower line-the horizontal line existing below the upper line and running toward the mastoid-temporal bone-the left and right sides of the skull Bone that forms part of the skull-parietal bone-bone that forms part of the skull from the top of the head (head of the head) to just behind the head-frontal bone-bone that forms the anterior part of the skull that exists between the left and right temporal bones -Occipital bone-The bone that forms the posterior part of the skull that exists between the left and right temporal bones-Temporal muscle-Muscle that covers almost the entire left and right temporal bone-Cap-shaped aponeurosis-Covers the skull toward each muscle Thin Fibrous Tissues ・Frontal Muscles-Muscles of Anterior Capsule Extending Anteriorly to Cover Anterior Skull ・Occipital Muscles-Muscles Covering Part of the Occipital Bone Above the Above Term Line-Lower Occipital Muscles- Muscle group consisting of multiple muscles attached to the skull base below the upper line

The meridian is a line that runs like a mesh so as not to connect the dots and the dots, and is distributed over the entire head, and is particularly concentrated in the frontal, occipital, and temporal muscles.

The meridian position existing in each zone varies depending on the size and shape of the patient's head, but is generally determined by applying the operator's finger to the patient's head and measuring the finger width.

More specifically, the width of the finger from the reference position present on the head, for example, the width of the thumb (one dimension in Oriental medicine), the width from the index finger to the ring finger (two dimensions in Oriental medicine), the index finger to the little finger The meridian positions distributed in each zone are determined by using the width (3 dimensions in Oriental medicine) as a measure of the distance to the meridian.

Further, the material forming the main body 1 of the surgical instrument is not particularly limited, and for example, metal, resin, or wood can be adopted.

When a resin is used as a material for forming the treatment device main body 1, the treatment device main body 1 is formed of a hard resin (for example, nylon resin) and the surface thereof is coated with a soft resin having elasticity (for example, vinyl resin). By forming it, it is possible to prevent careless damage to the scalp surface during the treatment.

In the present embodiment, the treatment device main body 1 is formed of nylon resin so that the treatment device as a whole has a feeling of weight, and the weight of the treatment device main body 1 facilitates grasping the treatment device and performing a treatment operation.

Further, in the main body 1 of the surgical instrument, the grip portion 2 is made thick, and the thickness of the bifurcated surgical portion 3 is gradually made thin from the base end to the distal end, thereby maintaining a heavy feeling in the whole surgical instrument. Can be made. Specifically, the thickness of the gripping portion is set to about 1.5 cm to 3.5 cm, and the thickness of the bifurcated operation portion 3 is formed to be about 0.3 cm to 3.5 cm so as to be thin from the base end to the tip.

If the rough surface 30 described above is formed on the entire outer surface of the practitioner main body 1, the friction resistance when the practitioner grips the grip portion 2 or the grip portion 4 with the palm is large, and the palm of the palm is not touched. It is possible to prevent the palm from being inadvertently slipped and displaced from the grip portion 2 or the grip portion 4 due to sweat or dryness.

In other words, since the roughening of the surface of the surgical instrument main body 1 is not performed on the entire outer surface of the surgical instrument main body 1, the subcutaneous tissue therapy surgical instrument A has unevenness on the rough surface on which the skin or scalp in contact with the surgical instrument main body 1 is applied. This makes it possible to perform an operation as if to grab.

Further, as shown in FIG. 17, the length of the rod-shaped or narrow-width grip portion 2 formed between the bifurcated operation portion 3 and the grip portion 4 is substantially equal to the width of the palm grip portion of the practitioner R. The length L1 is equivalent. Therefore, when the palm grip portion is rolled and the grip portion 2 is gripped, both end surfaces of the width of the palm grip portion come into close contact with the base portion 3a of the bifurcated operation portion 3 and the base portion 4a of the grip portion 4.

As shown in FIG. 3(a), not only the base 3a on the lower projection 6 side of the bifurcated treatment portion 3 but also the upper projection 5 is formed to bulge outward so that the upper projection 5 side is also formed. The base portion 3b may be formed, and the width of the rolled palm grip portion and the palm width when the rod-shaped grip portion 2 is gripped by the upper and lower base portions 3a and 3b are the same as the upper and lower base portions 3a and 3b of the bifurcated treatment portion 3. It is possible to closely contact the upper and lower base portions 4a and 4b of the grip portion 4 and fit between the base portions to more reliably obtain the gripping stress at the palm grip portion.

As another modification, as shown in the cross-sectional view of FIG. 14C, the rod-shaped grip portion 2 has a substantially flat plate shape, and its thickness (indicated by AA cross section in the drawing) is a bifurcated treatment portion. 3 and the grip portion 4 may be formed to have an enormous thickness portion shape as compared with the thick portion portions.

Further, as shown in FIGS. 14(a) and 14(b), the bifurcated treatment portion 3 is gradually sharpened toward the front end, and the frontmost end portion is rounded in plan view, and the front end is gradually increased in side view. If it is formed thinly, it can be accurately placed at the effective point of the treatment of the affected area, and the bifurcated treatment area 3 can be effectively applied to the subcutaneous tissue of the affected area without giving unnecessary excessive stimulation to the affected area. Can function.

Further, as shown in FIG. 3, the grip portion 4 has a substantially T-shape in a plan view, the T-shaped lateral side portion of the grip portion 4 abuts the palm of the practitioner during the treatment, and the T-shaped vertical side portion of the practitioner R does. It is configured to be held between fingers. When the bifurcated operation part 3 is pressed against the affected part, as shown in FIGS. 18 and 19, the grip part 4 is grasped and supported between the palm of the operator and the finger of the operator R.

Further, if the T-shaped lateral side portion of the grip portion 4 is formed in a curved shape so that the subcutaneous tissue (meridian) of the neck base portion can be pressed and stimulated, the grip portion 4 can be gripped by reversing and gripping the grip portion 2. If is located in the distal direction of the grip portion 2, it can be used for the treatment of the affected site subcutaneous tissue in the vicinity of the neck muscle, which is different from the occipital region, and the range of effective use of the treatment instrument body 1 can be expanded.

As another embodiment, as shown in FIG. 15, the upper and lower projections 5 and 6 of the bifurcated treatment part 3 are flat, and the flat tip edge is formed by forming a concave shape in the central portion of the flat surface. Left and right side projecting edge portions 5b, 5c, 6b, 6c may be formed.

Further, as another embodiment, as shown in FIG. 16, in the upper and lower projections 5 and 6 of the bifurcated treatment portion 3, the upper projection 5 is formed into a bifurcated shape that projects outward in the left and right directions from a flat thickness. You may spread and form two. That is, the subcutaneous tissue therapy apparatus A may be formed into a tripod shape by the same two upper protrusions 50 and 51 and one lower protrusion 6.

The two left and right upper protrusions 50, 61 are centered on the front end 6a position of the lower protrusion 6 in the thickness direction of the surgical instrument main body 1, and the front end 5b, 5c is arranged on the left and right sides from the central position. Is formed in a bifurcated shape outwardly in the thickness direction from the flat wall thickness.

[2. Clinical Embodiment Using Subcutaneous Tissue Therapy Device
Next, a clinical mode in which the subcutaneous tissue therapy apparatus A of the present invention is applied to the head of a patient will be specifically described.

As shown in FIG. 4 to FIG. 6 and FIG. 22, the patient sleeps on the bed according to the treatment of each segment. That is, when the first divisional band C1 and the second divisional band C2 are treated, the patient lies in a lying state with the occipital region facing upward as shown in FIG. 4, and when the third divisional band C3 is treated, the frontal area is shown as shown in FIG. The sleeping position is with the part facing upward, and the treatment of the fourth section band C4 is with the side lying with the temporal part facing upward, as shown in FIG.

In such a state, the operation is performed by pressing and stimulating the four-section zone with the subcutaneous tissue therapy apparatus A of the present invention in the direction of the arrow in FIG. 7, that is, in the direction perpendicular to the skull surface.

First, as shown in FIG. 17, the grasping portion 2 of the treatment instrument body 1 is grasped by the palm grasping portion, and the bifurcated treatment portion 3 is applied to a predetermined position on the head. In particular, the upper protrusion 5 of the bifurcated surgical portion 3 is located above the crown and the lower protrusion 6 is located below the neck and the like.

In the first section zone, the suboccipital muscle group M1 portion that covers the skull base B1 between the left and right temporal bones B4 and B4′ in layers, and the lower term line D1 in the head term line and the upper term line in the head term line. The curved surface area located between D2 and D2 is pressed. That is, as shown in FIG. 4 and FIG. 22, in the therapy in the first divisional band C1, the longer downward projection 6 extends across the boundary line between the first divisional band C1 and the second divisional band C2. Stimulation therapy is performed by setting the interval at which the short upper projection 5 abuts on the meridian of the second section zone C2 as the front end interval (tip interval) of the bifurcated operation part 3.

More specifically, the front end 5a of the upper protrusion 5 of the bifurcated treatment part 3 is attached to the second section strip so as to cross the upper line D2 that is the boundary line between the first section strip C1 and the second section strip C2. Of the cap-shaped aponeurosis M2 and the meridian distributed in the occipital muscle M3, and the front end 6a of the inferior projection 6 contacts the meridian distributed in the suboccipital muscle group M1 of the first section C1 and distributed in each area. Press the meridian to apply.

When positioning the treatment site, as shown in FIG. 4, first, the front end 5a of the upper projection 5 of the bifurcated treatment part 3 was pressed against the posterior part of the cap-shaped aponeurosis M2 of the second segment or the meridian of the occipital muscle M3. In this state, the subcutaneous tissue therapy apparatus A is moved upward (in the direction of the broken line arrow in FIG. 4), and the suboccipital muscle group M1 is tense via the cap-like aponeurosis M2 or occipital muscle M3.

Then, the downward projection 6 is pressed against the suboccipital muscle group M1 in a tensioned state in the first section C1 so that the bifurcation portion 3 grasps the meridians distributed in each section so that the meridians distributed in each section are reliably grasped. ..

Moreover, in this state, the driving force of the pressing stress of the grip portion 2 is used so as to be perpendicular to the head skull of the prone patient.

Particularly in the therapy in the first zone, along the curved surface area of the suboccipital muscle group M1 of the first sectional zone C1 and the posterior part of the cap-like aponeurosis M2 of the second sectional zone or the curved area of the occipital muscle M3. The bifurcated operation part 3 is laterally moved little by little in the lateral direction to cross the occipital region.

At the time of lateral movement, as shown in FIG. 20, the left and right seven meridian points (vessels on the meridian), the total of 14 left and right meridian points, respectively, of the first section band C1 and the second section band C2, are placed on the subcutaneous fat tissue. Press to perform stimulation.

Furthermore, at each point of the first section C1 and the second section C2, the upper projection 5 of the bifurcated surgical portion 3 is connected to the posterior part of the cap-like aponeurosis M2 of the second section C2 or the occipital muscle M3, and the lower projection 6 is formed. Are alternately or simultaneously applied to the suboccipital muscle group M1 of the first section zone C1.

That is, first, the posterior portion of the cap-like aponeurosis M2 or the occipital muscle M3 of the second segmental zone C2 is formed by the superior projection 5 of the bifurcated surgical treatment part 3, and the suboccipital muscle group M1 of the first segmented zone C1 is formed by the downward protrusion 6. In each of the pressing stimuli, as shown in FIG. 21, the grip portion 2 is the force point of the boom, the front end 5a of the shorter upper projection 5 is the fulcrum of the boom, and the front end 6a of the longer lower projection 6 is the action point of the boom. As a result, the affected area is pressed and stimulated.

Then, on the contrary, by stimulating the front end 6a of the elongated lower protrusion 6 as a fulcrum and the front end 5a of the upper protrusion 5 as an action point, the upper and lower protrusions 5 and 6 alternately serve as a fulcrum and a pressing action point. The operation is performed while changing the pressure stimulation point.

That is, at each point of the posterior portion of the cap-like aponeurosis M2 or the occipital muscle M3 of the second segmental zone C2 and the suboccipital muscle group M1 of the first segmental zone C1, the pressing force by the upper projection 5 is the lateral surface of the second half of the calvaria B2. The pressing force of the downward projection 6 acts on the upper cap type aponeurosis M2 or the occipital muscle M3 in the vertical direction to the suboccipital muscle group M1 on the outer bottom surface of the skull base B1.

As a result, the meridians distributed in the posterior portion of the cap-like aponeurosis M2 or the occipital muscle M3 of the second segment C2 are distributed perpendicularly to the side of the calvaria by the superior projection 5 and in the suboccipital muscle group M1 of the first segment C1. Will be sequentially pressed and stimulated along the transverse direction of the head so that the lower projection 6 pushes up the outer bottom surface of the skull base B1.

In this way, by making the lengths of the upper and lower projections 5 and 6 different so that the fulcrum and the action point of the upper and lower projections 5 and 6 are alternately displaced at the time of the operation, the surface of the skull is substantially spherical. The fulcrum and the action point can be exchanged with a small number of alternate pressing operations.

In particular, since the bifurcated portion 3 is applied to the affected area with the upper protrusion 5 as the fulcrum and the lower protrusion 6 as the point of action, the pressing force is applied to the deep part of the suboccipital muscle group M1 where a plurality of muscles are layered, that is, the lower layer. It can act on the muscles in position.

Next, in the second section zone C2, the occipital muscle M3 portion covering the posterior half of the calvaria B2 between the left and right temporal bones B4, B4′ and the cap aponeurosis M2 portion, and the upper term line D2 in the head term line. The surface curved area divided by the areas between the frontal muscle M4 and the left and right temporal bones B4 and B4′ is pressed. Specifically, as shown in FIG. 4, in the therapy in the second section C2, the front end of the bifurcated surgical treatment section 3 has an interval of abutting the front and back meridians scattered in the respective front and rear directions in the area of the second section C2. Stimulation is performed as an interval.

The axial direction of the pressing stress of the gripping portion 2 in this state is to be perpendicular to the second section band of the head skull of the prone patient, in other words, to be substantially horizontal to the second section band of the standing human head. To use.

That is, in the area of the second divisional band C2, the upper projection 5 is provided on the cap side aponeurosis M2 parietal side of the bifurcated operation part 3 in the anterior-posterior direction of the skull in accordance with the intervals of the antero-posterior meridians scattered in the antero-posterior direction. The lower projection 6 is applied to the frontal side of the cap-shaped aponeurosis M2, the occipital region of the cap-shaped aponeurosis M2, or the occipital muscle M3.

In positioning the treatment site, as shown in FIG. 4, first, the front end 5a of the upper protrusion 5 of the bifurcated treatment part 3 is pressed against the meridian of the cap-shaped aponeurosis M2 located on the parietal side, and subcutaneous tissue is placed. The therapeutic treatment device A is moved to the parietal region side (in the direction of the broken line arrow in the second section band in FIG. 4) to tense the cap-like aponeurosis M2 or occipital muscle M3 of the superior process 5.

Then, the downward projection 6 is pressed against the cap-like aponeurosis M2 or the occipital muscle M3 in a tensioned state in the second section band so that the meridians distributed in each section band are connected to the upper and lower projections 5 of the bifurcated operation part 3, Be sure to capture it as you grasp in 6.

In addition, in the therapy in the second section band C2, the bifurcated operation part 3 is laterally moved little by little in the area of the second section band C2 so as to traverse the anterior-posterior meridians scattered in the respective anteroposterior directions. The surface curved area of the divisional band C2 is traversed.

However, if necessary, it is possible to select only a predetermined point and perform the operation instead of the crossing operation. The predetermined operation point is a point suitable for effective subcutaneous tissue operation along the meridian (pot) in the second section zone C2, and this position is selected and specified by the operator's knowledge and experience.

Further, in the therapy in the second section zone, at each point of the curved surface area, the upper protrusion 5 of the bifurcated surgical portion 3 is used as the meridian distributed in the cap-like aponeurosis M2 on the parietal side, and the lower protrusion 6 is used as the occipital region. Pressing stress is alternately or simultaneously applied to the cap-like aponeurosis M2 on the side or the frontal region or the meridians distributed in the occipital muscle M3.

In particular, the meridians distributed in the cap-shaped aponeurosis M2 on the parietal side are distributed to the cap-shaped aponeurosis M2 on the occipital or frontal side or the occipital muscle M3 by the upper projection 5 of the bifurcated operation part 3. When the lower projection 6 is pressed and stimulated, as shown in FIG. 21, first, as shown in FIG. 21, the front end 5a of the short-shaped upper projection 5 is used as a fulcrum and the lower projection 6 is elongated. By pressing and stimulating the front end 6b as the point of action, and then by stimulating the front end 5a of the upper projection 5 as the point of action, the upper and lower protrusions 5 and 6 are alternately pressed and pressed. The operation is performed so as to cross the head while changing the pressure stimulus point so as to be the point of action.

Next, in the third division zone C3, the surface curved area defined by the frontal muscle M4 portion covering the front half of the calvaria B3 between the left and right temporal bones is pressed. That is, while the shorter upper protrusion is displaced along the boundary line D4 between the second divisional band C2 and the third divisional band C3, the longer lower protrusion abuts on the meridian of the third divisional band C3. The pressure stimulus is performed as the front end interval of the strip-shaped treatment section 3.

More specifically, as shown in FIG. 5, the upper protrusion front end 5a of the bifurcated operation part 3 is defined by a boundary line D3 between the second divisional zone C2 and the third divisional zone C3 (hatched aponeurosis M2 and frontal muscle M4). The lower meridian projection front end 6a is brought into contact with the meridian distributed in the frontal muscle M4 of the third section zone C3 to capture the meridian.

When positioning the treatment site, as shown in FIG. 5, the upper projection front end 5a of the bifurcated treatment portion 3 is first divided into the boundary line between the second division band and the third division band, as in the first and second division bands. The subcutaneous tissue therapy surgical instrument A is moved upward to the parietal region side while being pressed against D3, and the frontal muscle M4 of the third division zone is tensioned so as to be pulled up to the parietal region side.

Next, by pressing the downward projection 6 against the frontal muscle M4 in the tensioned state in the third section band C3, the meridian distributed in the boundary line D3 between the second section band C2 and the third section band C3 and the third section band C3. The two-pronged operation part 3 is used to grasp each other and to surely grasp each other.

The axial direction of the pressing stress of the grip portion 2 in this state is directed in the vertical direction with respect to the third section band C3 of the head skull of the patient lying on his back, in other words, in the horizontal transverse direction of the third section band of the standing human head. To use. That is, the bifurcated operation part 3 is applied so as to straddle between the meridians of the boundary line D3 between the second section band C2 and the third section band C3 and the frontal muscle M4 of the third section band C3.

Moreover, particularly in the therapy in the third section band, the longer lower projection 6 is displaced while the shorter upper projection 5 is displaced along the boundary line D3 between the second section band C2 and the third section band C3. The bifurcated operation part 3 is moved laterally little by little along the interval of contact with the meridian of C3 to cross the parietal region.

However, if necessary, it is possible to select only a predetermined point and perform the operation instead of the crossing operation. The predetermined operation point is a point suitable for effective subcutaneous tissue operation along the meridian in the third section zone, and this position is selected and specified by the operator R's knowledge and experience.

Further, in the therapy in the third section band, at each point of the second section band C2 and the third section band C3, as shown in FIG. 21, the upper protrusion 5 and the lower protrusion 6 of the bifurcated operation part 3 are respectively formed. Pressing stress is applied to and alternately or simultaneously.

In particular, when the boundary line D3 between the second section band C2 and the third section band C3 is pressed by the upper projection 5 of the bifurcated operation part 3 and the frontal muscle M4 of the third section band is pressed by the lower projection 6, Similarly to the case of the 1st and 2nd division zones, first, a short-shaped upper protrusion front end 5a is used as a fulcrum and a lower protrusion front end 6a is used as a point of action for stimulating pressure, and conversely, a longer lower protrusion front end 6a is used as a fulcrum. By performing pressure stimulation with 5 as an action point, the upper and lower protrusions 5 and 6 are alternately operated while changing the pressure stimulation point so that they serve as a pressure fulcrum and a pressure action point.

Next, in the fourth section zone C4, as shown in FIG. 6, the surface curved area defined by the temporal muscles M5 and M5' covering the left and right temporal bones B4 and B4' is pressed. That is, in the therapy in the fourth section zone C4, the shorter upper projection 5 is displaced along the boundary section D4 between the second section zone C2 and the fourth section zone C4 while the longer lower projection 6 is displaced into the fourth section. Stimulation therapy is performed on each of the left and right sides by setting the interval at which the band C4 abuts the meridian as the front end interval of the bifurcated operation part 3.

More specifically, the anterior projection front end 5a of the bifurcated treatment part 3 is located on the boundary line D4 between the second divisional zone C2 and the fourth divisional zone C4 (the boundary between the cap-like aponeurosis M2 and the temporalis muscle M5). The meridians distributed in each area are captured by contacting the distributed meridians and the front end 6a of the lower protrusion by contacting the meridians distributed in the frontal muscle M4 of the fourth section band C4.

At the time of positioning the treatment site, as shown in FIG. 6, first, the upper protrusion front end 5a of the bifurcated treatment part 3 is divided into the second division band C2 and the fourth division band C4, as in the first to third division bands. While being pressed against the boundary line D4, the subcutaneous tissue therapy apparatus A is moved upward to the parietal region side, and the temporal muscle M5 of the fourth section zone C4 is tensioned so as to be pulled up to the parietal region side.

Then, by pressing the downward projection 6 against the temporal muscle M5 in the tensioned state in the fourth section band C4, it is distributed on the boundary line D4 between the second section band C2 and the fourth section band C4 and the fourth section band C4. The meridians are surely grasped by grasping them with the bifurcated treatment part 3.

The axial direction of the pressing stress of the grip portion 2 in this state is the vertical direction with respect to the fourth division band C4 of the head skull of the prone patient with the head lying sideways, in other words, the fourth division band of the standing human head. Use it so that it faces horizontally. That is, the bifurcated operation part 3 is applied so as to straddle between the meridians of the boundary line D4 between the second section band C2 and the fourth section band C4 and the temporal muscle M5 of the fourth section band C4. ..

Particularly, in the therapy in the fourth section band C4, the shorter lower projection 6 is displaced while the shorter upper projection 5 is displaced along the boundary line D4 between the second section band C2 and the fourth section band C4. The bifurcated portion 3 is moved back and forth little by little along the interval of contact with the meridian, and the head is traversed in the front-back direction.

However, if necessary, it is possible to select only a predetermined point and perform the operation instead of the crossing operation. The predetermined operation point is a point suitable for effective subcutaneous tissue operation along the meridian in the fourth zone, and this position is selected and specified by the operator R's knowledge and experience.

Further, in the therapy in the fourth section band, the upper projection 5 and the lower projection 6 of the bifurcated operation part 3 are alternately or simultaneously pressed at each point of the second section band C2 and the fourth section band C4. Apply stress.

In particular, when the boundary line D4 between the second section band C2 and the fourth section band C4 is pressed by the upper protrusion 5 of the bifurcated operation part 3 and the temporal muscle M5 of the fourth section band is pressed by the lower protrusion 6, First, the short-sided upper protrusion front end 5a is used as a fulcrum and the lower protrusion front end 6a is used as an action point for pressure stimulation, and conversely, the longer lower protrusion front end 6a is used as a fulcrum for the upper protrusion 5 as an action point. The operation is performed while changing the pressing stimulus point so that the protrusions 5 and 6 alternately serve as the pressing fulcrum and the pressing action point.

As described above, the treatment is performed by the bifurcated treatment portion 3 in each area from the first division band to the fourth division belt. However, when the treatment device main body 1 is used, the grip portion having an enormous thickness portion is used. The bifurcated operation part 3 is vertically applied to the head of a patient who holds 2 in the palm of his left hand and lies prone.

At the same time, the palm of the right hand is applied to the rear end of the grip part 4 at the base of the bifurcated operation part 3, for example, the T-shaped lateral side part of the grip part, and the grip part 2 is pressed from the rear end direction while holding the grip part 2 with the left hand. The bifurcated operation part 3 is pressed against the patient's head through the medical treatment, and a prescribed subcutaneous tissue is subjected to therapeutic stimulation.

Moreover, since the upper protrusion 5 of the bifurcated treatment part 3 is projected along the axial direction of the grip portion 2, and the lower protrusion is provided at an angle of about 40° to 60° with respect to the axial direction of the grip portion, The pressing stress when applying the pressing stress in the axial direction of the grip portion 2 by vertically pressing the practitioner main body 1 against the segment band is more evenly transmitted to the affected area via the upper and lower projections 5 and 6, It is possible to stimulate the meridians and the like of the subcutaneous tissue in the area of the zone.

The material of the practitioner main body 1 is made of resin, and the functional surface of the bifurcated treatment part 3 is formed on the rough surface 30 so that the sliding friction is large, and is gradually sharpened toward the tip. The most distal portion is rounded in plan view and gradually thinned in the side view, so that the bifurcated surgical portion 3 is pressed against the affected area and the upper and lower protrusions 5 and 6 of different lengths are alternately fulcrum and point of action. When operated and used to perform each function, it is possible to perform a precise pressing operation with a feeling of weight, and the front and rear projections 5a and 6a, which serve as a fulcrum and a point of action, do not slip on the subcutaneous tissue without slipping off the affected area. It surely gives an effective stimulating action, and it becomes possible to perform modern disease therapy by stimulating subcutaneous tissue.

In addition, the T-shaped lateral portion of the curved grip portion 4 can also use the subcutaneous tissue at the base of the neck for pressure stimulation.

Further, the upper and lower protrusions 5 and 6 of the bifurcated treatment part 3 have a flat shape, and the flattened tip edge is formed in a concave shape at the central portion of the wall thickness, so that the flattened side surfaces have both right and left side projecting edge portions 5b, 5c and 6b. By forming 6c, it is also possible to apply a stable pressing force to the affected area by increasing the frictional resistance as much as there are many skin contacts on the surface of the skull.

[3. Measurement of Surface Roughness in Subcutaneous Tissue Therapy Device]
Next, in the subcutaneous tissue therapy apparatus according to this example, the surface roughness of the rough surface formed on the functional surface of the bifurcated operation part was verified.

The subcutaneous tissue therapy practitioner used for the verification was sandblasted to form a rough surface as the functional surface of the upper and lower projection front ends of the bifurcated treatment part. A rough surface having fine irregularities was formed. For comparison, a Kassa plate, which was made of hard plastic and had a flat shape and had a plurality of pressing protrusions at its edges, was used for the measurement.

The rough surface in the bifurcated treatment part of the subcutaneous tissue therapy surgical instrument is measured using a surface roughness/contour profile integrated measuring machine (Tokyo Seimitsu Surfcom5000DX Co., Ltd.) in a plan view with a measuring needle of the measuring instrument. The projection surface was traced from the outside to the bifurcated valley portion and from the bifurcated valley portion to the outside by performing the tracing a plurality of times (5 times each). The surface roughness was calculated as the arithmetic average height (Ra) according to JIS B6001-2001. Similarly, the surface roughness of the comparative brass plate was measured according to the above measuring method, and Ra was calculated.

As a result, the surface roughness of the roughened surface of the bifurcated treatment part in the subcutaneous tissue treatment device was detected in the range of Ra 10 μm to 35 μm, particularly in the range of Ra 15 μm to 30 μm. In addition, the appearance of the subcutaneous tissue therapy surgical instrument had a dull color due to the rough surface of the entire surgical instrument main body.

On the other hand, the brass plate for comparison had a glossy appearance, and the surface roughness was in the range of Ra 0.04 μm to 0.2 μm, which was the low value of the subcutaneous tissue therapy surgical instrument.

From such a result, in the subcutaneous tissue therapy apparatus according to the present invention, the convex portion derived from the rough surface having the surface roughness Ra of 10 μm to 35 μm is included in the skin tissue of the affected area so that the skin surface can be grasped without slipping. It was suggested that the operation device should be in a stable state and that the pressing force should be applied directly to the subcutaneous tissue from the convex part to give a pressing stimulus to the useful human function part to improve the manipulative treatment effect.

[4. Evaluation of Subcutaneous Tissue Therapy Device
Next, the subcutaneous tissue therapy operation device was evaluated. The instruments used for the evaluation are a surgical instrument S1 which is not subjected to rough surface treatment as a subcutaneous tissue therapy surgical instrument, a surgical instrument S2 which is subjected to a rough surface treatment with a surface roughness Ra of 10 μm to 35 μm, and also for comparison [3. Measurement of surface roughness in subcutaneous tissue therapy operating device] was used as a comparative brass plate.

Evaluation of the subcutaneous tissue therapy operating device was performed using each instrument [2. [Clinical Embodiment Using Subcutaneous Tissue Therapy Surgery Device] In the case of performing the pressing treatment described above, the viewpoint evaluation of the operability of the user and the viewpoint evaluation of the treatment feeling of the user were performed separately.

From the viewpoint of the user's operability, the five users will be evaluated on a scale of 1 to 5 by comprehensively judging the feeling of stability and grip of the instrument on the scalp surface of the user to be treated, It was decided that the higher the value, the higher the stability and grip. The results are shown in Table 1.

As can be seen from Table 1, it is shown that the practitioner S1 and the practitioner S2 are both highly stable and have a high grip for the practitioner as compared with the comparative braces.

In particular, the surgical instrument S2 that has been roughened is better in stability and grip during treatment than the surgical instrument S1 that has not been roughened, and it is easier to perform pressure treatment with less stress without discomfort. There were multiple answers.

Next, the viewpoint evaluation of the treatment feeling of the user was performed. The viewpoint evaluation of the user's feeling of treatment is performed by the above-mentioned five users who are in charge of the feelings transmitted from the tip of the device, that is, the feeling of being held by the protruding part of the device and the scalp thrusting operation by the device. The scalp's tension and the feeling of pressure on the scalp by the device are comprehensively evaluated, and a 5-level evaluation of 1 to 5 is made. The larger the value, the more the scalp is gripped, the feeling of tension, and the feeling of treatment such as pressure. I decided to have a high impression. The results are shown in Table 2.

As can be seen from Table 2, the practitioner S1 and the practitioner S2 have a high impression that the practitioner has a higher sense of treatment than the comparative braces, similarly to the viewpoint evaluation of the operability of the practitioner. It was shown to be.

In addition, the surgical instrument S2 that has been subjected to the rough surface treatment is more likely than the surgical instrument S1 that has not been subjected to the rough surface treatment to move the scalp in the divided band with fingers when the bifurcated treatment portion is pressed against the scalp surface. There were multiple answers that it was a feeling of being pressed while being grabbed.

From the above, the subcutaneous tissue therapy treatment apparatus according to the present embodiment plays a conventional role of simply “pushing” and “rubbing” like a “massage plate” as a conventional massager to provide a massage effect. It is fundamentally different from the one to be obtained, and it was suggested that the tissue underneath can be compressed without escaping from the pressing direction by "pushing", "turning" and "pulling" under "skin stretch condition". ..

In particular, in the subcutaneous tissue therapy operation device, the functional surface of the bifurcated operation part is formed into a rough surface that causes large sliding friction, so that the scalp can be grasped together with the subcutaneous tissue and the maximum can be crushed. It turns out that you can push it around after pulling it to the limit.

Thus, according to the subcutaneous tissue therapy surgical instrument of the present invention, the bifurcated surgical portion is used to perform the treatment while stimulating the affected area while tracing the spherical surface of the skull, and the direction in which the most pressing stress is applied to the skull. The vertical direction of the head of the patient lying prone, that is, the horizontal direction of the head in the standing position of the patient, is divided into 4 sections, and the 4 sections are subjected to subcutaneous tissue stimulation therapy from the posterior surface of the skull to the crown. There is an effect that can be.

Lastly, the description of each of the above-described embodiments is an example of the present invention, and other than each of the above-described embodiments, as long as it does not deviate from the technical idea of the present invention, depending on the design etc. It goes without saying that various modifications are possible.

A Subcutaneous Tissue Therapy Surgery Device 1 Surgery Device Body 2 Grip 3 Bifurcated Treatment 4 Grip 5 Upper Protrusion 6 Lower Protrusion

Claims (8)

The surgical instrument main body is composed of a grip portion and a bifurcated cervical head treatment portion formed at the tip of the grip portion and a grip portion formed at the rear end of the grip portion. The operation part is composed of a combination of a lower protrusion located closer to the neck and an upper protrusion located closer to the crown at the time of treatment,
The front end of the upper protrusion and the front end of the lower protrusion of the bifurcated treatment part are formed at intervals that can be placed across both edge lines of each division zone when the skull surface is divided into four division zones from the occipital region to the frontal region. ,
Moreover, of the four division bands that divide the skull from the occipital region to the frontal region,
The first segmented zone that divides the surface of the skull is the suboccipital muscle group portion that covers the skull base between the left and right temporal bones in layers, and the lower term line of the head line and the upper term line of the head line. Assuming surface curved areas located in between,
The second division zone that divides the surface of the skull is the occipital muscle portion covering the posterior half of the calvaria between the left and right temporal bones, and the cap-shaped aponeurosis portion, and between the superior term line and the frontal muscle in the cranial line. Assuming a surface curved area partitioned by each area of the area and the area of the left and right temporal bones,
The third zone that divides the surface of the skull assumes a curved surface area divided by the frontal muscle portion covering the anterior half of the calvaria between the left and right temporal bones,
The 4th division zone that divides the surface of the skull, assuming a curved surface area divided by the temporal muscle part covering the left and right temporal bones,
The distance between the upper and lower projections of the bifurcated part is
An interval in which the lower protrusion abuts on the meridian of the first division band and the upper protrusion abuts on the meridian of the second division band across the boundary line between the first division band and the second division band. An interval of contact with front and rear meridians scattered in the front-rear direction, an interval of contact of the lower protrusion with the meridian of the third partition band while displacing the upper protrusion along the boundary line between the second segment band and the third segment band, Subcutaneous tissue therapy apparatus characterized in that each interval is satisfied, such as an interval in which the lower protrusion abuts the meridian of the fourth segment band while displacing the upper protrusion along the boundary line between the segment band and the fourth segment band. .. The lower protrusion of the bifurcated treatment part is configured to project longer in the tip direction than the upper protrusion, and the distance between the front ends of the upper and lower protrusions of the bifurcated treatment part is determined by the first section band and the second section band. An interval in which the longer downward protrusions straddle the boundary line of and contact the meridian of the first section band and the shorter upper protrusions contact the meridian of the second section band, respectively, in the front-rear direction within the area of the second section band. Intervals of contact with scattered front and rear meridians, intervals of contact of long lower projections with meridians of the third section band while displacing shorter upper projections along the boundary line between the second and third section bands. , Satisfying the respective intervals, such as the interval at which the longer lower projection abuts the meridian of the fourth section band while displacing the shorter upper projection along the boundary line between the second section band and the fourth section band. The subcutaneous tissue therapy treatment device according to claim 1. The upper protrusion of the bifurcated surgical portion is projected along the axial direction of the grip portion, and the lower protrusion is provided at an angle of about 40° to 60° with respect to the axial direction of the grip portion. The subcutaneous tissue therapy treatment device according to claim 1 or 2. The upper and lower projections of the bifurcated portion to be treated have a flat shape, and the flat leading edge has a concave thickness at the central portion to form left and right projecting edges on both flat sides. The subcutaneous tissue therapy treatment device according to claim 3. When the rod-shaped gripping part between the bifurcated operation part and the grip part is grasped as the width of the palm grip of the practitioner, both widthwise end surfaces of the palm grip are in close contact with the bifurcated operation part and the grip part. 5. The subcutaneous tissue therapy surgical instrument according to claim 1, wherein The bifurcated portion is gradually sharpened toward the tip, and the distal end portion is rounded in a plan view and gradually thinned in a side view. 7. Substitute for acupressure subcutaneous tissue therapy in place of acupressure. The subcutaneous tissue according to any one of claims 1 to 6, wherein the functional surface of the bifurcated treatment portion formed at the front end of the grip portion is formed into a rough surface so that sliding friction is large. Therapy unit. The subcutaneous tissue therapy surgical instrument according to any one of claims 1 to 7, wherein the surgical instrument main body is made of a resin, and is configured to maintain a feeling of weight during a surgical operation and to perform a stable surgical operation. ..

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